Herbal Formula Danggui-Shaoyao-San Promotes Neurogenesis and Angiogenesis in Rat Following Middle Cerebral Artery Occlusion

被引:35
|
作者
Ren, Changhong [1 ,2 ]
Wang, Brian [2 ]
Li, Ning [1 ]
Jin, Kunlin [2 ]
Ji, Xunming [1 ,3 ]
机构
[1] Capital Med Univ, Inst Hypoxia Med, Xuanwu Hosp, Beijing 100053, Peoples R China
[2] Univ N Texas, Hlth Sci Ctr, Dept Pharmacol & Neurosci, Ft Worth, TX 76107 USA
[3] Capital Med Univ, Xuanwu Hosp, Dept Neurosurg, Beijing 100053, Peoples R China
来源
AGING AND DISEASE | 2015年 / 6卷 / 04期
关键词
Ischemic stroke; Dangui-Shaoyao San; Angiogenesis; Neurogenesis; TOKI-SHAKUYAKU-SAN; NITRIC-OXIDE; ENHANCES NEUROGENESIS; STROKE MECHANISMS; GROWTH-FACTOR; IMPAIRMENT; EXPRESSION; RECOVERY;
D O I
10.14336/AD.2014.1126
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Current studies demonstrated that traditional Chinese herbal formula Danggui-Shaoyao-San (DSS) is not only used for the treatment of menstrual disorder, but has also found its use in neurological diseases. However, the neuroprotective role of DSS on ischemia-induced brain injury is still unclear. The aim of the present study is to explore the effect of DSS in ischemic brain injury. Total 30 adult female Sprague-Dawley rats underwent 90 min transient middle cerebral artery occlusion (MCAO). DSS (600 mg/kg) was administered through the intragastric route at the time of reperfusion and then performed every day thereafter until sacrifice. Results showed that DSS treatment significantly improved neurobehavioral outcomes (N=10 per group, P<0.05). Immunohistochemical staining showed that microvessel density in the perifocal region of DSS-treated rats was significantly increased compared to the saline-treated group (N=4 per group, P<0.01). Similarly, the numbers of BrdU(+)/DCX+ cells in the subventricular zone were increased in DSS-treated rats compared to the saline-treated group (P<0.05). Furthermore, we demonstrated that DSS treatment activated vascular endothelial growth factor (N=4 per group, P<0.05) and promoted eNOS phosphorylation (N=4 per group, P<0.05). Thus, we concluded that DSS promoted focal angiogenesis and neurogenesis, and attenuated ischemia-induced brain injury in rats after MCAO, suggesting that DSS is a potential drug for ischemic stroke therapy.
引用
收藏
页码:245 / 253
页数:9
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